atrial fibrillation
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: (1)Japanese patient with anticoagulant therapy for non valvular atrial fibliration (2)Patient with 20 years old and older (3)Patient signed Informed consent
Exclusion criteria
Exclusion criteria: (1)Patient recieved or will recieve catheter ablation during follow up. (2)Patient recieved catheter ablation for atrial fibliration in the past 6 month. (3)In patient with cancer, not noticed of cancer at the time of informed consent. (4)Patient judged unsuitable for the study by prncipal investigator or subinvetigator
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| We investigate the new events of stroke and/or systemic embolism by the type of anticoagulant and therapy (medicine vs non medicine) during follow-up period of 12M after informed cocent. | — |
Secondary
| Measure | Time frame |
|---|---|
| Death(cardiovascular death/non-cardiovascular death), stroke(ischemic/hemorrhagic/unclassified), systemic embolism, cardiovascular event(acute myocardial infarction/unstable angina), hemorrhagic event (intracranial bleeding except hemorrhagic stroke, gastrointestinal bleeding), adverse event, others | — |
Countries
Japan
Contacts
Tokyo Medical and Dental University Heart Rhythm Center